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临床试验/CTIS2023-503602-37-00
CTIS2023-503602-37-00进行中(未招募)1 期

Effect at 3 months of early empagliflozin initiation in cardiogenic shock patients on mortality, rehospitalization, left ventricular ejection fraction and renal function. A randomized multicentric open trial. (EMPASHOCK) - 2021PI218

CHRU De Nancy0 个研究点目标入组 164 人开始时间: 2023年12月12日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
164

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Adult patients =18 years old hospitalized in critical cardiac unit care or Intensive care unit for a cardiogenic shock, Patient on catecholamine for more than 12 hours., Person affiliated to a social security scheme

排除标准

  • GFR< 20 ml/min/1.73m2., Women of childbearing age without effective contraception, Type 1 diabete patient, Person referred to in Articles 10, 31, 32, 33 and 34 of EU Regulation 536/2014 (Pregnant woman, parturient or breastfeeding mother, Minor (not emancipated), Adult person subject to a legal protection measure (guardianship, curatorship, safeguard of justice)), Chronic dialysis, Patient on SGLT2 inhibitors prior to admission to intensive care unit or CCU, Known allergy to SGLT2 inhibitors or to any of its excipients (in particular, patients with hereditary disorders of galactose intolerance, total lactase deficiency or glucose or galactose malabsorption syndrome), Patients on lithium., Patient in shock for another cause or moribund (SAPS2> 90)., Specific cardiogenic shock context: a. cardiac transplant patient or on transplant list. b. of peripartum, adrenergic, valvular, restrictive, post embolic heart disease. c. caused by a conduction/rhythm disorder of non-ischemic etiology. d. related to cardiotropic drug intoxication. e. secondary to a cardiocirculatory arrest with more than 25 min of low flow or more than 5 min of no flow before recovery of a stable cardiac activity., Patient undergoing VA-ECMO at admission (before or in whom implantation is imminent (less than 3 hours)).

研究者

发起方
CHRU De Nancy

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